EP2213303A1 - Pharmaceutical composition for treatment of cataract - Google Patents
Pharmaceutical composition for treatment of cataract Download PDFInfo
- Publication number
- EP2213303A1 EP2213303A1 EP08839364A EP08839364A EP2213303A1 EP 2213303 A1 EP2213303 A1 EP 2213303A1 EP 08839364 A EP08839364 A EP 08839364A EP 08839364 A EP08839364 A EP 08839364A EP 2213303 A1 EP2213303 A1 EP 2213303A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- formula
- lower alkyl
- hydrogen
- cataract
- vap
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/426—1,3-Thiazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0048—Eye, e.g. artificial tears
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/12—Ophthalmic agents for cataracts
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/38—Nitrogen atoms
- C07D277/44—Acylated amino or imino radicals
- C07D277/46—Acylated amino or imino radicals by carboxylic acids, or sulfur or nitrogen analogues thereof
Definitions
- the present invention relates to a pharmaceutical composition for the treatment of cataract, which comprises an effective amount of a VAP-1 inhibitor.
- VAP-1 The vascular adhesion protein-1 (hereinafter to be abbreviated as VAP-1) is amine oxidase (semicarbazide sensitive amine oxidase, SSAO) abundantly existing in human plasma, which shows a remarkably increased expression in vascular endothelium and vascular smooth muscle in the inflammatory lesion.
- VAP-1 gene was cloned in 1998, and VAP-1 was reported to be a membrane protein which, as an adhesion molecule, controls rolling and migration of lymphocytes and NK cells under the expression control of inflammatory cytokine.
- amine to be the substrate is unknown, it is considered to be methylamine produced in any part in the living body.
- VAP-1 inhibitor a thiazole derivative having a particular structure, which is a VAP-1 inhibitor, is used for the prophylaxis or treatment of VAP-1 related diseases such as macular edema, vascular hyperpermeable disease and the like.
- VAP-1 related diseases such as macular edema, vascular hyperpermeable disease and the like.
- the present invention aims to provide a pharmaceutical composition for the treatment of cataract, which comprises an effective amount of a VAP-1 inhibitor.
- the present inventors have conducted intensive studies and found that a VAP-1 inhibitor is effective for the treatment of cataract, which resulted in the completion of the present invention.
- the present invention provides the following.
- R 1 is acyl
- X is a divalent residue derived from optionally substituted thiazole
- Y is a bond, lower alkylene, lower alkenylene or -CONH-
- Z is the formula
- Q is -S- or -NH-;
- R 3 is hydrogen, lower alkyl, lower alkylthio or -NH-R 4 wherein R 4 is hydrogen, -NH 2 or lower alkyl, or a derivative thereof, or a pharmaceutically acceptable salt thereof.
- R 2 is the formula:
- G is a bond, -NHCOCH 2 - or lower alkylene;
- R 2 is as defined above.
- R 2 is as defined above.
- the pharmaceutical composition for the treatment of cataract which comprises an effective amount of a VAP-1 inhibitor of the present invention, can be used for the prophylaxis or treatment of the disease.
- the present invention provides a pharmaceutical composition for the treatment of cataract, which comprises an effective amount of a VAP-1 (vascular adhesion protein-1) inhibitor (hereinafter to be sometimes referred to as the composition of the present invention).
- the cataract in the present invention is a disease wherein clouding develops in the crystalline lens due to various causes, resulting in vision loss.
- cataract also includes pre-cataract stages observed as increased intensity of scattering light in the crystalline lens, colored crystalline lens, nuclear sclerosis and the like.
- the composition of the present invention can be used for the treatment of any cataract irrespective of the cause, particularly for the prophylaxis, namely, prevention of the onset.
- Such cataract includes, for example, age-related cataract, traumatic cataract, nutritional cataract, diabetic cataract, drug (steroid etc.)-induced cataract, atopic cataract, complicated cataract, radiation cataract and the like.
- treatment in the present invention encompasses any management of disease including prophylaxis, treatment, relief and prevention of aggravation.
- R 1 is acyl
- X is a divalent residue derived from optionally substituted thiazole
- Y is a bond, lower alkylene, lower alkenylene or -CONH-
- Z is the formula
- Q is -S- or -NH-;
- R 3 is hydrogen, lower alkyl, lower alkylthio or -NH-R 4 wherein R 4 is hydrogen, -NH 2 or lower alkyl.
- lower is used to mean a group having a carbon number of 1 to 6, preferably 1 to 4, unless otherwise specified.
- lower alkyl examples include a straight chain or branched chain alkyl having a carbon number of 1 to 6 (e.g., methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, tert-pentyl and hexyl) and the like.
- C 1 -C 4 alkyl is more preferable.
- lower alkylene examples include a straight chain or branched chain alkylene having a carbon number of 1 to 6 (e.g., methylene, ethylene, trimethylene, tetramethylene, propylene, ethylidene and propylidene) and the like. Among these, C 1 -C 4 alkylene is more preferable.
- C 2 -C 4 alkenylene is more preferable.
- the above-mentioned lower alkenylene may be an E-form or Z-form.
- the compound of the present invention encompasses any stereoisomer wherein the lower alkenylene moiety is an E-structure or Z-structure.
- lower alkylthio is a group wherein a sulfur atom is bonded to the alkyl moiety, which is straight chain or branched chain, the above-mentioned lower alkyl group having a carbon number of 1 to 6, and examples thereof include methylthio, ethylthio, propylthio, isopropylthio, butylthio, isobutylthio, sec-butylthio, tert-butylthio, pentylthio, tert-pentylthio, hexylthio and the like.
- alkylcarbonyl examples include alkylcarbonyl wherein the alkyl moiety has a carbon number of 1 to 6 [that is, the alkyl moiety is C 1 -C 6 alkyl of the above-mentioned "lower alkyl”] (e.g., acetyl, propionyl, butyryl, isobutyryl, valeryl, isovaleryl, pivaloyl, hexanoyl and heptanoyl) and the like.
- lower alkyl e.g., acetyl, propionyl, butyryl, isobutyryl, valeryl, isovaleryl, pivaloyl, hexanoyl and heptanoyl
- aryl examples include C 6 -C 10 aryl (e.g., phenyl and naphthyl) and the like, where the “aryl” may be substituted by 1 to 3 substituents and the position of substitution is not particularly limited.
- aralkyl examples include aralkyl wherein the aryl moiety has a carbon number of 6 to 10 [that is, the aryl moiety is C 6 -C 10 aryl of the above-mentioned "aryl”], and the alkyl moiety has a carbon number of 1 to 6 [that is, the alkyl moiety is C 1 -C 6 alkyl of the above-mentioned "lower alkyl”] (e.g., benzyl, phenethyl, 1-naphthylmethyl, 2-naphthylmethyl, 3-phenylpropyl, 4-phenylbutyl and 5-phenylpentyl) and the like.
- amino of the “optionally substituted amino” may be substituted by 1 or 2 substituents, and the substituent may be a protecting group.
- the "optionally substituted amino” is represented by the formula -NR 5a R 5b .
- R 5a or R 5b examples include lower alkyl, acyl, alkoxycarbonyl, aryl, aralkyl, cyclo(lower)alkyl, cyclo(lower)alkoxycarbonyl, sulfuryl, sulfinyl, phosphoryl, heterocyclic group and the like, each of which is unsubstituted or optionally substituted, and hydrogen.
- the lower alkyl, acyl, alkoxycarbonyl, aryl and aralkyl are as defined above or below.
- cyclo(lower)alkyl examples include cycloalkyl having a carbon atom and having a carbon number of 3 to 6 (e.g., cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl).
- cyclo(lower)alkoxycarbonyl examples include cycloalkoxycarbonyl wherein the cycloalkyl moiety has a carbon atom and having a carbon number of 3 to 6 (e.g., cyclopropyloxycarbonyl, cyclobutyloxycarbonyl, cyclopentyloxycarbonyl, cyclohexyloxycarbonyl).
- R 5a and R 5b may be the same or different.
- heterocycle examples include “aromatic heterocycle” and “non-aromatic heterocycle”.
- aromatic heterocycle examples include a 5- to 10-membered aromatic heterocycle containing, besides carbon atoms, 1 to 3 hetero atoms selected from nitrogen, oxygen and sulfur atom and the like, for example, thiophene, furan, pyrrole, imidazole, pyrazole, thiazole, isothiazole, oxazole, isoxazole, pyridine, pyridazine, pyrimidine, pyrazine and the like.
- non-aromatic heterocycle examples include a 5- to 10-membered non-aromatic heterocycle containing, besides carbon atoms, 1 to 3 hetero atoms selected from nitrogen, oxygen and sulfur atom and the like, for example, pyrrolidine, imidazoline, pyrazolidine, pyrazoline, piperidine, piperazine, morpholine, thiomorpholine, dioxolane, oxazolidine, thiazolidine, triazolidine and the like.
- acyl examples include alkylcarbonyl, arylcarbonyl and the like.
- alkylcarbonyl examples include alkylcarbonyl wherein the alkyl moiety has 1 to 6 carbon atoms [that is, the alkyl moiety is C 1 -C 6 alkyl of the above-mentioned “lower alkyl”] (e.g., acetyl, propionyl, butyryl, isobutyryl, valeryl, isovaleryl, pivaloyl, hexanoyl and heptanoyl) and the like.
- arylcarbonyl examples include arylcarbonyl wherein the aryl moiety has 6 to 10 carbon atoms [that is, the aryl moiety is C 6 -C 10 aryl of the above-mentioned “aryl”] (e.g., benzoyl and naphthoyl) and the like.
- alkoxycarbonyl examples include alkyloxycarbonyl, aralkyloxycarbonyl and the like.
- alkyloxycarbonyl examples include alkyloxycarbonyl wherein the alkyl moiety has a carbon number of 1 to 10 (e.g., methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, butoxycarbonyl, isobutoxycarbonyl, sec-butoxycarbonyl, tert-butoxycarbonyl, pentyloxycarbonyl, tert-pentyloxycarbonyl, hexyloxycarbonyl etc.) and the like.
- alkyloxycarbonyl wherein the alkyl moiety has a carbon number of 1 to 10 (e.g., methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, butoxycarbonyl, isobutoxycarbonyl, sec-butoxycarbonyl, tert-butoxycarbonyl, pentyloxycarbonyl, tert-pentyloxycarbonyl,
- aralkyloxycarbonyl examples include aralkyloxycarbonyl wherein the aryl moiety has a carbon number of 6 to 10 [that is, the aryl moiety is C 6 -C 10 aryl of the above-mentioned "aryl”], and the alkyl moiety has a carbon number of 1 to 6 [that is, the alkyl moiety is C 1 -C 6 alkyl of the above-mentioned "lower alkyl”] (e.g., benzyloxycarbonyl, phenethyloxycarbonyl, 1-naphthylmethyloxycarbonyl, 2-naphthylmethyloxycarbonyl, 3-phenylpropyloxycarbonyl, 4-phenylbutyloxycarbonyl and 5-phenylpentyloxycarbonyl etc.) and the like.
- divalent residue derived from the optionally substituted thiazole examples include
- the "thiazole” may have a substituent, and the position of substitution is not particularly limited.
- substituents of the above-mentioned “optionally substituted thiazole” include a group described in the following (1) - (12) and the like.
- the position of substitution on aryl or heterocycle may be any and is not particularly limited.
- Preferable "substituent" of the above-mentioned “optionally substituted thiazole” is methylsulfonylbenzyl, sulfamoylbenzyl (e.g., 4-sulfamoylbenzyl) and the like.
- the position of substitution of the methylsulfonyl group, sulfamoyl group and the like is not particularly limited.
- R 1 is alkylcarbonyl (which is as defined above), and more preferable example is acetyl.
- thiazole moiety of the "divalent residue derived from optionally substituted thiazole" for X
- Y include lower alkylene (which is as defined above), and ethylene and the like are particularly preferable.
- a preferable example of Z is the following formula (II):
- R 2 is a group of the following formula:
- R 2 is a group of the following formula:
- R 2 in the formula (I) includes the following formula (III)
- J-L-M (III) wherein J is -NR 2a -, -NR 2a -CO-, -(CH 2 ) n - or -(CH 2 ) n CO- (wherein R 2a is hydrogen, lower alkyl, or acyl; n is an integer of 0 to 6); L is -NR 2b - wherein R 2b is hydrogen, lower alkyl, alkoxycarbonyl or acyl; and M is optionally substituted amino.
- J-L-M moiety is a group wherein J is a bond, -NH-CO- or -(CH 2 ) n CO- wherein n is an integer of 0 to 2; L is -NH- or -N(CH 3 )-; and, M is optionally substituted amino.
- J-L-M moiety examples include -CO-NH-NH 2 , -CH 2 -CO-NH-NH 2 , -CH 2 -CO-NH-NH-CH 3 , -CH 2 -CO-N(CH 3 )-NH 2 , -CH 2 -CO-NH-NH-C 2 H 5 , -CH 2 -CO-NH-N(CH 3 ) 2 , -(CH 2 ) 2 -CO-NH-NH 2 , -NH-CO-NH-NH 2 , -NH-NH-NH 2 , -CH 2 -NH-NH 2 , -(CH 2 ) 2 -NH-NH 2, -(CH 2 ) 3 -NH-NH 2 and the like.
- R 1 is preferably alkylcarbonyl
- X is preferably a divalent residue derived from thiazole optionally substituted by methylsulfonylbenzyl.
- the compound represented by the formula (I) in the present invention is preferably N- ⁇ 4-[2-(4-hydrazinocarbonylmethylphenyl)ethyl]-1,3-thiazol-2-yl ⁇ acetamide, N-(4- ⁇ 2-[4-(2- ⁇ [amino(imino)methyl]amino ⁇ ethyl)phenyl]ethyl ⁇ -1,3-thiazol-2-yl)acetamide or the like.
- the invention encompasses all enantiomers and diastereomers.
- the "derivative" in the present invention is intended to encompass all compounds derived from the original compound.
- the VAP-1 inhibitor particularly a compound represented by the formula (I) of the present invention and a derivative thereof of the present invention can also be converted to a pharmaceutically acceptable salt.
- the pharmaceutically acceptable salt in the present invention is not particularly limited as long as it is a nontoxic pharmaceutically acceptable general salt, and a salt with an inorganic or organic base, acid addition salt and the like can be mentioned.
- the salt with an inorganic or organic base include alkali metal salt (e.g., sodium salt, potassium salt etc.), alkaline earth metal salt (e.g., calcium salt, magnesium salt etc.), ammonium salt, and amine salt (e.g., triethylamine salt, N-benzyl-N-methylamine salt etc.) and the like.
- the acid addition salt examples include salts derived from mineral acid (e.g., hydrochloric acid, hydrobromic acid, hydroiodic acid, phosphoric acid, metaphosphoric acid, nitric acid and sulfuric acid), and salts derived from organic acid (e.g., tartaric acid, acetic acid, citric acid, malic acid, lactic acid, fumaric acid, maleic acid, benzoic acid, glycol acid, gluconic acid, succinic acid and arylsulfonic acid (e.g., p-toluenesulfonic acid)) and the like.
- mineral acid e.g., hydrochloric acid, hydrobromic acid, hydroiodic acid, phosphoric acid, metaphosphoric acid, nitric acid and sulfuric acid
- organic acid e.g., tartaric acid, acetic acid, citric acid, malic acid, lactic acid, fumaric acid, maleic acid, benzoic acid, glycol acid, gluconic
- the compound represented by the formula (I) and a derivative thereof, and a pharmaceutically acceptable salt thereof of the present invention can be used as medicaments and the like in the form of a prodrug.
- prodrug means any compounds that can be converted to a VAP-1 inhibitor in the body after administration.
- the prodrug may be any pharmaceutically acceptable prodrug of a composition of the present invention.
- the compound represented by the formula (I) of the present invention and a derivative thereof, pharmaceutically acceptable salts thereof, and prodrugs thereof can be produced by a known method ( W02004/067521 , WO2006/011631 , WO2006/028269 ), a combination thereof and the like.
- composition of the present invention can be administered by any route.
- administration route include systemic administration (e.g., oral administration or injection administration), topical administration (e.g., instillation, eye ointment) and the like.
- the mode of administration of the composition of the present invention may be appropriately determined according to whether the application to cataract is for a prophylactic purpose or treatment purpose, and the like.
- Preferable administration route is topical administration to the eye.
- composition of the present invention is preferably administered rapidly to an administration subject such as a mammal, particularly human, after diagnosis of having a risk of cataract and before the onset thereof (prophylactic treatment). Alternatively, it is administered rapidly after the onset of cataract in the administration subject (therapeutic treatment).
- the treatment plan can be appropriately determined according to the kind of an active ingredient to be used, dose, administration route, cause, level of awareness of cataract where necessary, and the like.
- the administration route may be an appropriately effective one and one or more routes can be used. Accordingly, the above-mentioned administration routes are mere exemplifications free of any limitation.
- the dosage (dose) of the treatment agent of the present invention for a subject of administration such as animal including human, particularly human, is an amount sufficient to provide a desired response in the subject of administration for a reasonable period of time.
- the dosage is appropriately determined according to various factors including the strength of the active ingredient to be used, age, species, symptom, disease state, body weight and severity of disease of the subject of administration, the route, timing and frequency of the administration and the like.
- the dosage can also be appropriately controlled according to the route, timing and frequency of the administration and the like. Depending on the symptom or disease state, a long-term treatment involving plural times of administration may be necessary.
- the dosage and administration schedule can be determined by a technique within the ordinary range known to those of ordinary skill in the art.
- the prophylaxis or treatment is started from a dosage lower than the optimal dosage of the compound. Thereafter, the dosage is gradually increased until the optimal effect is obtained under the circumstances.
- the daily dosage of a VAP-1 inhibitor as an active ingredient is generally about 0.03 ng/kg body weight/day - about 300 mg/kg body weight/day, preferably about 0.003 ⁇ g/kg body weight/day - about 10 mg/kg body weight/day. Both a single administration and 2 to 4 times of administration per day can be employed before, between or after meals.
- the composition can be administered in a sustained manner.
- composition of the present invention preferably contains a "pharmaceutically acceptable carrier" and, as an active ingredient, a VAP-1 inhibitor in an amount sufficient to prevent or therapeutically treat cataract.
- the carrier may be any as long as it is generally used as a medicament, and is not particularly limited except for when it is limited by physicochemical items to be considered (e.g., solubility and lack of reactivity to the compound) and administration route.
- the amount of the VAP-1 inhibitor in the composition of the present invention may vary depending on the formulation of the composition. It is generally 0.00001 - 10.0 wt%, preferably 0.001 - 5 wt%, relative to the whole composition.
- the administration form (dosage form) of the composition of the present invention is not particularly limited and can be administered in various forms to achieve a desired VAP-1 inhibitory action.
- the composition of the present invention can be formulated into an oral or parenteral preparation by using the composition of the present invention solely or in combination with a pharmaceutically acceptable additive such as carrier, diluent and the like.
- a pharmaceutically acceptable additive such as carrier, diluent and the like.
- the characteristics and property of the preparation are determined by the solubility and chemical property of the active ingredient, selected administration route and standard pharmaceutical practice.
- Examples of the preparation to be used for oral administration include solid dosage forms (e.g., capsule, tablet, powder), liquid forms (e.g., solution or suspension) and the like.
- the preparation to be used for parenteral administration examples include injection, drip and eye drop, which are in the form of a sterile solution or suspension, eye ointment and the like.
- the solid oral preparation may contain conventional excipients (e.g., lactose, sucrose, magnesium stearate, resin, and like materials) and the like.
- the liquid oral preparation can contain various aromatic, colorant, preservative, stabilizer, solubilizer, suspending agent and the like.
- the parenteral preparation is, for example, an aseptic aqueous or nonaqueous solution or suspension, and can contain particular various preservatives, stabilizer, buffer agent, solubilizer, suspending agent and the like. Where necessary, the solution may be made isotonic by adding an additive such as saline or glucose.
- composition of the present invention may contain other pharmaceutically active compound as long as it does not inhibit the effect of the invention.
- composition of the present invention can be administered simultaneously with other pharmaceutically active compound as long as the effect of the present invention is not impaired.
- the "simultaneous administration” means administration of other pharmaceutically active compound before, simultaneously (e.g., in the same preparation or in different preparation), or after administration of the composition of the present invention, by the same or different administration route.
- examples of other pharmaceutically active compound include corticosteroid, prednisone, methylprednisone, dexamethasone, triamcinolone acetinide or non-corticosteroid anti-inflammatory compound (e.g., ibuprofen or flurbiprofen).
- vitamin and mineral e.g., zinc, antioxidant such as carotenoid (e.g., xanthophyll carotenoid-like zeaxanthin or lutein)
- trace nutrition and the like can be recited.
- the present invention provides use of a VAP-1 inhibitor for the production of a pharmaceutical composition for the treatment of cataract.
- the present invention also provides a method for the treatment of cataract, which comprises a method comprising a step of administering, to a test subject in need of the treatment, a pharmaceutical composition comprising a VAP-1 inhibitor in an amount sufficient to treat the disease of the test subject or suppress the development or progression of cataract.
- the starting compounds to be used in the following Production Example can be produced by a known method ( WO2004/067521 , W02006/011631 , WO2006/028269 ) and the like.
- the Production Example of the VAP-1 inhibitor to be used in the present invention is shown below.
- Rats (Crj: Wistar, male, 5-week-old) were purchased, grouped after acclimation for 6 days, and fasted for 20 hr. After the fasting, Streptosotocin (hereinafter STZ, 50 mg/kg (2 mL/kg)) was administered to the tail vein. After 24 hr from the STZ administration, the blood glucose level was measured, and the rats with blood glucose level of not less than 250 mg/dL were considered as STZ induced diabetic rat (measurement tool: ACCU-CHEK Aviva, Roche Diagnostics K.K.) (group 2 - group 4).
- STZ Streptosotocin
- test substance 1 N- ⁇ 4-[2-(4-hydrazinocarbonylmethylphenyl)ethyl]-1,3-thiazol-2-yl ⁇ acetamide (compound described in Production Example)
- test substance 2 N-(4- ⁇ 2-[4-(2- ⁇ [amino(imino)methyl]amino ⁇ ethyl)phenyl]ethyl ⁇ -1,3-thiazol-2-yl)acetamide (compound described in WO2006/011631 , Production Example 25)
- test substances 1 and 2 suppress the onset of cataract.
- Rats (Crj: Wistar, male, 3-week-old) were purchased and, from the next day (Day 0), a mixture of a powder feed (CRF-1, Oriental Yeast Co., ltd.) and 30% of galactose (special grade, Wako Pure Chemical Industries, Ltd., Lot# 075-00035) was freely given. From Day 0, test substance 1 was repetitively administered orally. Vehicle (dissolution liquid) was administered to group 1 and test substance 1 (0.5%) was administered to group 2 at a dose of 2 mL/kg once per day, and the presence or absence of the onset of cataract was observed for 20 days.
- Vehicle dissolution liquid
- test substance 1 0.5%) was administered to group 2 at a dose of 2 mL/kg once per day, and the presence or absence of the onset of cataract was observed for 20 days.
- Table 3 group medicament concentration number of rats (eyes) group 1 dissolution liquid - 6(12) group 2 test substance 1 0.5 wt% 6(12)
- dissolution liquid 0.5% methylcellulose solution test substance 1: N- ⁇ 4-[2-(4-hydrazinocarbonylmethylphenyl)ethyl]-1,3-thiazol-2-yl ⁇ acetamide (compound described in Production Example)
- test substance 1 suppresses the onset of cataract.
- This application is based on a patent application No. 2007-272993 filed in Japan, the contents of which are incorporated in full herein by this reference.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007272993 | 2007-10-19 | ||
PCT/JP2008/068853 WO2009051223A1 (ja) | 2007-10-19 | 2008-10-17 | 白内障処置のための医薬組成物 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP2213303A1 true EP2213303A1 (en) | 2010-08-04 |
EP2213303A4 EP2213303A4 (en) | 2011-12-28 |
Family
ID=40567484
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP08839364A Withdrawn EP2213303A4 (en) | 2007-10-19 | 2008-10-17 | PHARMACEUTICAL COMPOSITION FOR THE TREATMENT OF CATARACT |
Country Status (8)
Country | Link |
---|---|
US (1) | US20100210697A1 (enCached4) |
EP (1) | EP2213303A4 (enCached4) |
JP (1) | JPWO2009051223A1 (enCached4) |
KR (1) | KR20100096094A (enCached4) |
CN (2) | CN101903045B (enCached4) |
CA (1) | CA2702885A1 (enCached4) |
TW (1) | TW200927100A (enCached4) |
WO (1) | WO2009051223A1 (enCached4) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011075430A1 (en) * | 2009-12-14 | 2011-06-23 | University Of Massachusetts | Methods of inhibiting cataracts and presbyopia |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI437986B (zh) | 2008-01-31 | 2014-05-21 | R Tech Ueno Ltd | 噻唑衍生物及使用該衍生物作為vap-1抑制劑之用途 |
TWI490214B (zh) * | 2008-05-30 | 2015-07-01 | 艾德克 上野股份有限公司 | 苯或噻吩衍生物及該等作為vap-1抑制劑之用途 |
MX2012004777A (es) | 2009-10-30 | 2012-06-01 | Nestec Sa | Metodos para mantener la salud de los ojos y mejorar enfermedades oftalmicas en caninos. |
CA3086105A1 (en) | 2012-05-02 | 2013-11-07 | Boehringer Ingelheim International Gmbh | Substituted 3-haloallylamine inhibitors of ssao and uses thereof |
ES2727293T3 (es) | 2013-03-14 | 2019-10-15 | Univ Massachusetts | Métodos de inhibición de cataratas y presbicia |
CN108348494A (zh) | 2015-11-13 | 2018-07-31 | 马萨诸塞大学 | 用于抑制白内障和老花眼的含peg的双官能分子 |
EP3386494A1 (en) | 2015-12-07 | 2018-10-17 | Benevolentai Cambridge Limited | Vap-1 inhibitors for treating pain |
CN107915752B (zh) * | 2017-11-14 | 2018-09-18 | 牡丹江医学院 | 一种治疗白内障的药物及其制备方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006011631A2 (en) * | 2004-07-27 | 2006-02-02 | Astellas Pharma Inc. | Thiazole derivatives having vap-1 inhibitory activity |
US20070191408A1 (en) * | 2004-01-30 | 2007-08-16 | Faron Pharmaceuticals Oy | Compositions useful especially for treatment or prevention of metabolic syndrome |
WO2009001857A1 (ja) * | 2007-06-25 | 2008-12-31 | R-Tech Ueno, Ltd. | 低酸素または虚血に伴う眼疾患用組成物 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4442118A (en) * | 1981-07-23 | 1984-04-10 | Ayerst, Mckenna & Harrison, Inc. | Aldose reductase inhibition by 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetic acid |
KR20120030601A (ko) | 2003-01-27 | 2012-03-28 | 아스텔라스세이야쿠 가부시키가이샤 | 티아졸 유도체 및 vap-1 저해제로서의 용도 |
CA2520957C (en) * | 2003-03-31 | 2013-08-06 | Sucampo Ag | Method for treating vascular hyperpermeable disease |
CA2549029A1 (en) * | 2004-01-30 | 2005-08-11 | Faron Pharmaceuticals Oy | Compositions for treatment or prevention of metabolic syndrome |
KR101206319B1 (ko) * | 2004-03-18 | 2012-11-29 | 가부시키가이샤 아루떼꾸 우에노 | 티아졸 유도체를 포함하는 수성 조성물 |
WO2006028269A2 (en) | 2004-09-09 | 2006-03-16 | Astellas Pharma Inc. | Thiazole derivatives having vap-1 ihibitory activity |
-
2008
- 2008-10-17 JP JP2009538168A patent/JPWO2009051223A1/ja active Pending
- 2008-10-17 KR KR1020107010849A patent/KR20100096094A/ko not_active Application Discontinuation
- 2008-10-17 US US12/738,588 patent/US20100210697A1/en not_active Abandoned
- 2008-10-17 CN CN2008801213455A patent/CN101903045B/zh not_active Expired - Fee Related
- 2008-10-17 WO PCT/JP2008/068853 patent/WO2009051223A1/ja active Application Filing
- 2008-10-17 TW TW097139853A patent/TW200927100A/zh unknown
- 2008-10-17 CN CN2013100232593A patent/CN103120690A/zh active Pending
- 2008-10-17 CA CA2702885A patent/CA2702885A1/en not_active Abandoned
- 2008-10-17 EP EP08839364A patent/EP2213303A4/en not_active Withdrawn
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070191408A1 (en) * | 2004-01-30 | 2007-08-16 | Faron Pharmaceuticals Oy | Compositions useful especially for treatment or prevention of metabolic syndrome |
WO2006011631A2 (en) * | 2004-07-27 | 2006-02-02 | Astellas Pharma Inc. | Thiazole derivatives having vap-1 inhibitory activity |
WO2009001857A1 (ja) * | 2007-06-25 | 2008-12-31 | R-Tech Ueno, Ltd. | 低酸素または虚血に伴う眼疾患用組成物 |
Non-Patent Citations (3)
Title |
---|
A. W. STITT: "The Maillard Reaction in Eye Diseases", ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, vol. 1043, no. 1, 1 June 2005 (2005-06-01) , pages 582-597, XP55012445, ISSN: 0077-8923, DOI: 10.1196/annals.1338.066 * |
POKUPEC RAJKO ET AL: "Advanced glycation endproducts in human diabetic and non-diabetic cataractous lenses", GRAEFE'S ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, SPRINGER VERLAG, XX, vol. 241, no. 5, 1 May 2003 (2003-05-01), pages 378-384, XP002616571, ISSN: 0721-832X, DOI: 10.1007/S00417-002-0616-2 [retrieved on 2003-04-16] * |
See also references of WO2009051223A1 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011075430A1 (en) * | 2009-12-14 | 2011-06-23 | University Of Massachusetts | Methods of inhibiting cataracts and presbyopia |
Also Published As
Publication number | Publication date |
---|---|
JPWO2009051223A1 (ja) | 2011-03-03 |
EP2213303A4 (en) | 2011-12-28 |
TW200927100A (en) | 2009-07-01 |
CN101903045B (zh) | 2013-03-13 |
KR20100096094A (ko) | 2010-09-01 |
CN103120690A (zh) | 2013-05-29 |
US20100210697A1 (en) | 2010-08-19 |
WO2009051223A1 (ja) | 2009-04-23 |
CA2702885A1 (en) | 2009-04-23 |
CN101903045A (zh) | 2010-12-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2213303A1 (en) | Pharmaceutical composition for treatment of cataract | |
KR101206319B1 (ko) | 티아졸 유도체를 포함하는 수성 조성물 | |
EP2252604B1 (en) | Thiazole derivative and use thereof as vap-1 inhibitor | |
ES2766326T3 (es) | Composiciones, formulaciones y métodos para tratar enfermedades oculares | |
KR101154163B1 (ko) | 티아졸 유도체 및 vap-1 저해제로서의 용도 | |
JP2972377B2 (ja) | カテコール誘導体、その薬学的に許容しうる塩およびエステルならびにそれらを含有する医薬組成物 | |
EP2611415B1 (en) | Adenosine a1 agonists for the treatment of glaucoma and ocular hypertension | |
US5753681A (en) | Treatment and prophylaxis of pancreatitis | |
EP2599498A1 (en) | Composition for ophthalmic disease associated with hypoxia or ischemia |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20100511 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT RO SE SI SK TR |
|
AX | Request for extension of the european patent |
Extension state: AL BA MK RS |
|
DAX | Request for extension of the european patent (deleted) | ||
A4 | Supplementary search report drawn up and despatched |
Effective date: 20111124 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: C07D 277/46 20060101ALI20111118BHEP Ipc: C07D 277/20 20060101ALI20111118BHEP Ipc: A61P 43/00 20060101ALI20111118BHEP Ipc: A61P 27/12 20060101ALI20111118BHEP Ipc: A61K 31/426 20060101ALI20111118BHEP Ipc: A61K 45/00 20060101AFI20111118BHEP |
|
17Q | First examination report despatched |
Effective date: 20121115 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
18D | Application deemed to be withdrawn |
Effective date: 20140501 |